Methodological Advancements in Pharmaceutical Industries
As developers and manufacturers of life-saving products, the world’s leading pharmaceutical companies play an important eccentric in improving access to medicine for the world’s poor. Through their own initiatives and in collaboration with other relevant stakeholders such as multi-lateral organizations, governments and the global health community, these companies are increasingly helping to address the admittance to medicine challenge. In order to suitably capture the industry’s progress in line with society’s evolving expectations, the Access to Medicine Index methodology is systematically reviewed every two years. While maintaining as much consistency as possible for the purpose of trend analysis, the methodology is adjusted where needed.
- Analytical Chemistry
- Technological Innovations
- Optimization Techniques in Pharmaceutical Formulation and Processing
- Synthesis of heterocyclic compounds
- Technologies in Drug Delivery
- Separation Processes in Chemical Manufacturing Industries.
- Quality Control, Quality Assurance and Regulatory Filings
- Advances and applications in HPLC Techniques
- Spectroscopy in Pharmaceutical Analysis
- Design and Analysis in Chemical Research
- Aqueous and Non-Aqueous Titrimetric Method
- Modern Pharmaceutical Analysis
- Degradation and Impurity Analysis of Different Dosage Forms
- Assay Methods Based on Separation Techniques
- Industrial Pharmacy and Pharmacy Practices
- Errors in Pharmaceutical Analysis
- Pharmaceutical Methods and Innovations
Related Conference of Methodological Advancements in Pharmaceutical Industries
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Methodological Advancements in Pharmaceutical Industries Conference Speakers
Recommended Sessions
- Chemical and Pharmaceutical Engineering
- Drug Design And Development
- Drug Formulation Procedures
- Drug Product Manufacturing
- Biomarkers in Drug Design
- Clinical Trails & Biotherapeutics
- Computer Aided Drug Design (CADD)
- Drug Delivery and Distribution
- Entrepreneur Investment
- Innovative Drug Discovery and Nanotechnology
- Medicinal Chemistry and Drug Discovery Advancements
- Methodological Advancements in Pharmaceutical Industries
- Molecular Modelling in Drug Designing
- Novel Drug Delivery System
- Novel Drug Target Approaches
- Pharmaceutical Regulatory Affairs
- Pharmacokinetics and Pharmacodynamics
- Pharmacology and Toxicology
- Pre-Formulation & Formulation Aspects
- Traditional Medicine Design
- Types of Formulations
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- Regulatory Requirements for Pharmaceuticals - PHARMACEUTICAL SCIENCES 2026 (Italy)
- Regulatory Science and Clinical Trial Innovations - Euro Antibiotics 2025 (Netherlands)
- Regulatory updates on Biosimilars - Eurobiosimilars 2026 (Italy)
- Rehabilitation and Physical Therapy in Pain - Pain Management 2026 (France)
- Risk-Based Monitoring and Trial Optimization - Clinical Trials-2026 (UK)
- Safety Pharmacology - Pharmacology 2026 (Italy)
- Safety Reporting in Early Phase Trials - Clinical Trials-2026 (UK)
- Semi-Solid Dosage Forms - Formulations 2025 (France)
- Sexually Transmitted Bacterial Infections and Resistance Trends - Euro Antibiotics 2025 (Netherlands)
- Signal Prioritization and Management Techniques - Clinical Trials-2026 (UK)
- Single-Use Technologies in Production - Biologics Meet 2026 (UK)
- Site Management Innovation - Clinical Research 2026 (UK)
- Smart Drug Delivery Systems - Formulations 2025 (France)
- Solid Dosage Forms - Formulations 2025 (France)
- Stem Cell and Genetic Clinical Research - Clinical Research 2026 (UK)
- Stewardship Programs in Human and Animal Health - Euro Antibiotics 2025 (Netherlands)
- Structure-Based Drug Design and Molecular Docking - Euro MedChem and CADD 2025 (France)
- Supply Chain Management - Pharmaceuticals-2025 (France)
- Sustainable Antibiotic Practices and Global Policy - Euro Antibiotics 2025 (Netherlands)
- Sustainable Biologics Manufacturing - Biologics Meet 2026 (UK)
- Synthetic and Bioorganic Chemistry - PHARMACEUTICAL CHEMISTRY 2025 (France)
- Synthetic and Green Medicinal Chemistry - Euro MedChem and CADD 2025 (France)
- Systems Pharmacology and Drug Modeling - Euro Pharmacology 2025 (France)
- Target Identification and Validation - Euro MedChem and CADD 2025 (France)
- Targeted Drug Delivery and Nanomedicine in Infectious Diseases - Euro Antibiotics 2025 (Netherlands)
- Targeted Therapies - Personalizedmedicine-2025 (Switzerland)
- Technology in Pharma Sciences - MedTech-2025 (Switzerland)
- Telemedicine - Personalizedmedicine-2025 (Switzerland)
- The Role of CROs in Clinical Trial Execution - Clinical Trials-2026 (UK)
- Toxicological Impacts of Air and Water Pollution - Euro Pharmacology 2025 (France)
- Toxicology - Pharmacology 2026 (Italy)
- Toxicology and Safety Pharmacology - Pharmacology-2025 (Germany)
- Toxicology: Mechanisms and Risk Assessment - Euro Pharmacology 2025 (France)
- Translational Research - Personalizedmedicine-2025 (Switzerland)
- Types of Formulations - Formulations 2025 (France)
- USFDA Approved Biosimilars - Eurobiosimilars 2026 (Italy)
- Vaccine Development Against Bacterial Pathogens - Euro Antibiotics 2025 (Netherlands)
- Vaccines & Immunotherapy - Pharma Expo-2026 (Thailand)
- Veterinary Pharmacology - Pharmacology-2025 (Germany)